OLYMPUS URETERO. & CIRCON ACMI URETERO. GUIDE— 510(k) K896821

Name: FDA 510(k) clearance K896821
Creator: U.S. Food and Drug Administration
Published: 1990-02-09

Substantially Equivalent

North American Sterilization & Packaging Co.

FDA 510(k) clearance K896821 for OLYMPUS URETERO. & CIRCON ACMI URETERO. GUIDE, Substantially Equivalent on 1990-02-09. Applicant: North American Sterilization & Packaging Co.. Device class: 1.

Clearance details

Applicant: North American Sterilization & Packaging Co.
Product code: Code KOQ
Device class: Class 1
Regulation: 21 CFR 872.3410
Advisory panel: Dental
Date received: 1989-12-04
Decision date: 1990-02-09
Decision: Substantially Equivalent
Clearance type: Traditional
Location: Sparta, NJ, US

Download summary PDF View on FDA.gov ↗

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